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PUBMED FOR HANDHELDS

Journal Abstract Search


124 related items for PubMed ID: 5170137

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  • 3. [A family of familial amyloidosis with cerebellar ataxia and pyramidal tract sign--clinical and genetic study (author's transl)].
    Kobayashi T, Nakagawa S, Oguchi K, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1978 Sep; 18(9):515-24. PubMed ID: 709971
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  • 7. [Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders].
    Mettey R, Hoppeler A, Gil R.
    J Genet Hum; 1981 Sep; 29(3):227-34. PubMed ID: 7334346
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  • 10. [Electroretinography and electroencephalography in spinocerebellar degenerations].
    Stanescu B, Wawernia E.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Jan; 33(1):43-8. PubMed ID: 4267723
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  • 13. [Family with hereditary polyneuropthy assoicated with pyramidal signs].
    Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M.
    Rinsho Shinkeigaku; 1976 Sep; 16(9):642-8. PubMed ID: 1034548
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  • 14. [2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy].
    Kato Y, Takayama K, Tsujiyama Y, Kaga T, Satowa H.
    No To Shinkei; 1970 Oct; 22(10):1201-8. PubMed ID: 5536190
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  • 15. [Amyotrophic form of a spinocerebellar degeneration. Anatomoclinical study and nosological discussion].
    Boudouresques J, Toga M, Khalil R, Gosset A, Vigouroux RA, Pellissier JF.
    Rev Neurol (Paris); 1971 Jul; 125(1):25-38. PubMed ID: 5138162
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  • 16. A simple method for evoking dorsiflexion of the hallux in pyramidal lesions.
    Serbănescu T.
    Rev Roum Neurol Psychiatr; 1974 Jul; 11(3):219-25. PubMed ID: 4846957
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  • 19. [Familial atrophic form of spinocerebellar ataxia].
    Gaj T, Grendus-Tota B.
    Neurol Neurochir Pol; 1973 Jul; 7(5):679-83. PubMed ID: 4763007
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  • 20. Spinocerebellar ataxia with neural myatrophy.
    Hopf HC, Volles E.
    Neuropadiatrie; 1971 Jul; 3(1):97-105. PubMed ID: 5170970
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